The functions of animal microRNAs

Untitled work

Bartel (2004) · doi:10.1016/s0092-8674(04)00045-5 · Cited by 34,714

The C. elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14

Lee, R. C., Feinbaum, R. L., & Ambros, V. (1993) · Cell · doi:10.1016/0092-8674(93)90529-y · Cited by 12,948

Prediction of Mammalian MicroRNA Targets

Lewis, B. P., Shih, I.-H., Jones-Rhoades, M. W., Bartel, D. P., & Burge, C. B. (2003) · Cell · doi:10.1016/s0092-8674(03)01018-3 · Cited by 5,199

The 21-nucleotide let-7 RNA regulates developmental timing in Caenorhabditis elegans

Reinhart, B. J., Slack, F. J., Basson, M., Pasquinelli, A. E., Bettinger, J. C., Rougvie, A. E., Horvitz, H. R., & Ruvkun, G. (2000) · Nature · doi:10.1038/35002607 · Cited by 4,989

Identification of Novel Genes Coding for Small Expressed RNAs

Lagos-Quintana, M., Rauhut, R., Lendeckel, W., & Tuschl, T. (2001) · Science · doi:10.1126/science.1064921 · Cited by 4,956

Posttranscriptional regulation of the heterochronic gene lin-14 by lin-4 mediates temporal pattern formation in C. elegans

Wightman, B., Ha, I., & Ruvkun, G. (1993) · Cell · doi:10.1016/0092-8674(93)90530-4 · Cited by 4,292

MicroRNA targets in Drosophila

Enright, A. J., John, B., Gaul, U., Tuschl, T., Sander, C., & Marks, D. S. (2003) · Genome Biology · doi:10.1186/gb-2003-5-1-r1 · Cited by 3,597

Identification of tissue-specific microRNAs from mouse

Lagos-Quintana, M., Rauhut, R., Yalcin, A., Meyer, J., Lendeckel, W., & Tuschl, T. (2002) · Current Biology · doi:10.1016/s0960-9822(02)00809-6 · Cited by 3,355

An Abundant Class of Tiny RNAs with Probable Regulatory Roles in Caenorhabditis elegans

Lau, N. C., Lim, L. P., Weinstein, E. G., & Bartel, D. P. (2001) · Science · doi:10.1126/science.1065062 · Cited by 3,345

MicroRNAs Modulate Hematopoietic Lineage Differentiation

Chen, C.-Z., Li, L., Lodish, H. F., & Bartel, D. P. (2004) · Science · doi:10.1126/science.1091903 · Cited by 3,257

Prediction of potential disease-associated microRNAs using structural perturbation method

Zeng, X., Liu, L., Lü, L., & Zou, Q. (2018) · Bioinformatics · doi:10.1093/bioinformatics/bty112 · Cited by 235

Recent progress in microRNA delivery for cancer therapy by non-viral synthetic vectors

Wang, H., Jiang, Y., Peng, H., Chen, Y., Zhu, P., & Huang, Y. (2014) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2014.10.031 · Cited by 235

Transgenic miR132 Alters Neuronal Spine Density and Impairs Novel Object Recognition Memory

Hansen, K. F., Sakamoto, K., Wayman, G. A., Impey, S., & Obrietan, K. H. (2010) · PLoS ONE · doi:10.1371/journal.pone.0015497 · Cited by 235

MicroRNA Mirn122a Reduces Expression of the Posttranscriptionally Regulated Germ Cell Transition Protein 2 (Tnp2) Messenger RNA (mRNA) by mRNA Cleavage1

Yu, Z., Raabe, T. D., & Hecht, N. B. (2005) · Biology of Reproduction · doi:10.1095/biolreprod.105.040998 · Cited by 235

MicroRNA-146a expresses in interleukin-17 producing T cells in rheumatoid arthritis patients

Niimoto, T., Nakasa, T., Ishikawa, M., Okuhara, A., Izumi, B., Deie, M., Suzuki, O., Adachi, N., & Ochi, M. (2010) · BMC Musculoskeletal Disorders · doi:10.1186/1471-2474-11-209 · Cited by 235

miR-21: an oncomir on strike in prostate cancer

Folini, M., Gandellini, P., Longoni, N., Profumo, V., Callari, M., Pennati, M., Colecchia, M., Supino, R., Veneroni, S., Salvioni, R., et al. (2010) · Molecular Cancer · doi:10.1186/1476-4598-9-12 · Cited by 234

Characterization and biological function of milk‐derived miRNAs

Golan‐Gerstl, R., Shiff, Y. E., Moshayoff, V., Schecter, D. R., Leshkowitz, D., & Reif, S. S. (2017) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201700009 · Cited by 234

lncRNAs: Insights into their function and mechanics in underlying disorders

Li, X., Wu, Z., Fu, X., & Han, W. (2014) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2014.04.002 · Cited by 233

Heterochronic Genes and the Nature of Developmental Time

Moss, E. G. (2007) · Current Biology · doi:10.1016/j.cub.2007.03.043 · Cited by 234

Regulation of cyclin dependent kinase 6 by microRNA 124 in medulloblastoma

Pierson, J., Hostager, B., Fan, R., & Vibhakar, R. (2008) · Journal of Neuro-Oncology · doi:10.1007/s11060-008-9624-3 · Cited by 233

Phosphorylation of Argonaute 2 at serine-387 facilitates its localization to processing bodies

Zeng, Y., Sankala, H. M., Zhang, X., & Graves, P. R. (2008) · Biochemical Journal · doi:10.1042/bj20080599 · Cited by 233

The maintenance of memory plasma cells

Khodadadi, L., Cheng, Q., Radbruch, A., & Hiepe, F. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00721 · Cited by 232

miTarget: microRNA target gene prediction using a support vector machine

Kim, S., Nam, J., Rhee, J., Lee, W.-J., & Zhang, B.-T. (2006) · BMC Bioinformatics · doi:10.1186/1471-2105-7-411 · Cited by 232

HGIMDA: Heterogeneous graph inference for miRNA-disease association prediction

Chen, X., Yan, C. C., Zhang, X., You, Z., Huang, Y., & Yan, G. (2016) · Oncotarget · doi:10.18632/oncotarget.11251 · Cited by 232

Nonsense-mediated decay in genetic disease: Friend or foe?

Miller, J. N., & Pearce, D. A. (2014) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2014.05.001 · Cited by 231

Early Second-Trimester Serum MiRNA Profiling Predicts Gestational Diabetes Mellitus

Zhao, C., Dong, J., Jiang, T., Shi, Z., Yu, B., Zhu, Y., Chen, D., Xu, J., Huo, R., Dai, J., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0023925 · Cited by 230

Regulation of cholesterol homeostasis

Goedeke, L., & Fernandez-Hernando, C. F. (2011) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-011-0857-5 · Cited by 232

A three-step pathway comprising PLZF/miR-146a/CXCR4 controls megakaryopoiesis

Labbaye, C., Spinello, I., Quaranta, M. T., Pelosi, E., Pasquini, L., Petrucci, E., Biffoni, M., Nuzzolo, E. R., Billi, M., Foà, R., et al. (2008) · Nature Cell Biology · doi:10.1038/ncb1741 · Cited by 230

MicroRNA 132 Regulates Nutritional Stress-Induced Chemokine Production through Repression of SirT1

Strum, J. C., Johnson, J. H., Ward, J. M., Xie, H., Feild, J. A., Hester, A. G., Alford, A., & Waters, K. M. (2009) · Molecular Endocrinology · doi:10.1210/me.2009-0117 · Cited by 229

MicroRNA Expression Aberration as Potential Peripheral Blood Biomarkers for Schizophrenia

Lai, C.-Y., Yu, S.-L., Hsieh, M. H., Chen, C.-H., Chen, H.-Y., Wen, C.-C., Huang, Y.-H., Hsiao, P.-C., Hsiao, C. K., Liu, C.-M., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0021635 · Cited by 228

miR-484 regulates mitochondrial network through targeting Fis1

Wang, K., Long, B., Jiao, J.-Q., Wang, J., Liu, J., Li, Q., & Li, P. (2012) · Nature Communications · doi:10.1038/ncomms1770 · Cited by 230

MicroRNAs as Effectors of Brain Function with Roles in Ischemia and Injury, Neuroprotection, and Neurodegeneration

Saugstad, J. A. (2010) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2010.101 · Cited by 229

Micro‐RNA signature of the epithelial–mesenchymal transition in endometrial carcinosarcoma

Castilla, M. Á., Moreno‐Bueno, G., Romero‐Pérez, L., de Vijver, K. K. V., Biscuola, M., López‐García, M. Á., Prat, J., Matías‐Guiu, X., Cano, A., Oliva, E., et al. (2010) · The Journal of Pathology · doi:10.1002/path.2802 · Cited by 228

miR-34/449 miRNAs are required for motile ciliogenesis by repressing CP110

Song, R., Walentek, P., Sponer, N., Klimke, A., Lee, J. S., Dixon, G., Harland, R., Wan, Y., Lishko, P., Lize, M., et al. (2014) · Nature · doi:10.1038/nature13413 · Cited by 228

Important aspects of Toll-like receptors, ligands and their signaling pathways

Chang, Z. L. (2010) · Inflammation Research · doi:10.1007/s00011-010-0208-2 · Cited by 228

Liver-Specific MicroRNA miR-122 Enhances the Replication of Hepatitis C Virus in Nonhepatic Cells

Chang, J., Guo, J., Jiang, D., Guo, H., Taylor, J. M., & Block, T. M. (2008) · Journal of Virology · doi:10.1128/jvi.02575-07 · Cited by 228

LRSSLMDA: Laplacian Regularized Sparse Subspace Learning for MiRNA-Disease Association prediction

Chen, X., & Li, H. (2017) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1005912 · Cited by 228

Lipid and Polymer-Based Nanoparticle siRNA Delivery Systems for Cancer Therapy

Mainini, F., & Eccles, M. R. (2020) · Molecules · doi:10.3390/molecules25112692 · Cited by 228

Identification of functional microRNAs released through asymmetrical processing of HIV-1 TAR element

Ouellet, D. L., Plante, I., Landry, P., Barat, C., Janelle, M.-E., Flamand, L., Tremblay, M. J., & Provost, P. (2008) · Nucleic Acids Research · doi:10.1093/nar/gkn076 · Cited by 226

Polyphenols in the treatment of autoimmune diseases

Khan, H. Z., Sureda, A., Belwal, T., Çetinkaya, S., Süntar, I. P., Tejada, S., Devkota, H. P., Ullah, H., & Aschner, M. (2019) · Autoimmunity Reviews · doi:10.1016/j.autrev.2019.05.001 · Cited by 227

BAFF and APRIL support chronic lymphocytic leukemia B-cell survival through activation of the canonical NF-κB pathway

Endo, T., Nishio, M., Enzler, T., Cottam, H. B., Fukuda, T., James, D. F., Karin, M., & Kipps, T. J. (2006) · Blood · doi:10.1182/blood-2006-06-027755 · Cited by 225

Ovarian cancer cell invasiveness is associated with discordant exosomal sequestration of Let-7 miRNA and miR-200

Kobayashi, M., Salomón, C., Tapia, J., Illanes, S. E., Mitchell, M. D., & Rice, G. E. (2014) · Journal of Translational Medicine · doi:10.1186/1479-5876-12-4 · Cited by 225

MicroRNA‐196: critical roles and clinical applications in development and cancer

Chen, C., Zhang, Y., Zhang, L., Weakley, S. M., & Yao, Q. C. (2010) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2010.01219.x · Cited by 224

Micro RNAs of Epstein-Barr Virus Promote Cell Cycle Progression and Prevent Apoptosis of Primary Human B Cells

Seto, E., Moosmann, A., Grömminger, S., Walz, N., Grundhoff, A. T., & Hammerschmidt, W. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1001063 · Cited by 224

One-step ultrasensitive detection of microRNAs with loop-mediated isothermal amplification (LAMP)

Li, C., Li, Z., Jia, H., & Yan, J. (2010) · Chemical Communications · doi:10.1039/c0cc03957h · Cited by 224

The MicroRNA Signature of Mouse Spermatozoa Is Substantially Modified During Epididymal Maturation1

Nixon, B., Stanger, S. J., Mihalas, B. P., Reilly, J. N., Anderson, A. L., Tyagi, S., Holt, J. E., & McLaughlin, E. A. (2015) · Biology of Reproduction · doi:10.1095/biolreprod.115.132209 · Cited by 224

MicroRNA–target pairs in the rat kidney identified by microRNA microarray, proteomic, and bioinformatic analysisPreprint

Tian, Z., Greene, A. S., Pietrusz, J. L., Matus, I. R., & Liang, M. (2008) · Genome Research · doi:10.1101/gr.6587008 · Cited by 224

An updated role of microRNA-124 in central nervous system disorders: a review

Sun, Y., Luo, Z.-M., Guo, X.-M., Su, D.-F., & Liu, X. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00193 · Cited by 223

MicroRNA: Implications for Alzheimer Disease and other Human CNS Disorders

Maes, O. C., Chertkow, H. M., Wang, E., & Schipper, H. M. (2009) · Current Genomics · doi:10.2174/138920209788185252 · Cited by 223

Argonaute 2 Complexes Selectively Protect the Circulating MicroRNAs in Cell-Secreted Microvesicles

Li, L., Zhu, D., Huang, L., Zhang, J., Bian, Z., Chen, X., Liu, Y., Zhang, C., & Zen, K. (2012) · PLoS ONE · doi:10.1371/journal.pone.0046957 · Cited by 223

Substrate requirements for let-7 function in the developing zebrafish embryo

Kloosterman, W. P., Wienholds, E., Ketting, R. F., & Plasterk, R. H. A. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw173 · Cited by 223

Targeting Foam Cell Formation in Atherosclerosis: Therapeutic Potential of Natural Products

Wang, D., Yang, Y., Lei, Y., Tzvetkov, N. T., Liu, X., Yeung, A. W. K., Xu, S., & Atanasov, A. G. (2019) · Pharmacological Reviews · doi:10.1124/pr.118.017178 · Cited by 223

Molecular mechanisms of natural killer cell activation in response to cellular stress

Chan, C. J., Smyth, M. J., & Martinet, L. (2013) · Cell Death and Differentiation · doi:10.1038/cdd.2013.26 · Cited by 222

Identification of 188 conserved maize microRNAs and their targets

Zhang, B., Pan, X., & Anderson, T. A. (2006) · FEBS Letters · doi:10.1016/j.febslet.2006.05.063 · Cited by 222

Embryonic Stem Cell-Specific miR302-367 Cluster: Human Gene Structure and Functional Characterization of Its Core Promoter

Jesus, A. B.-D., Romero‐López, C., Lucena-Aguilar, G., Melen, G. J., Sánchez, L., Ligero, G., Berzal‐Herranz, A., & Menéndez, P. R. (2008) · Molecular and Cellular Biology · doi:10.1128/mcb.00398-08 · Cited by 222

A journey into the world of insect lipid metabolism

Toprak, U., Hegedus, D. D., Doğan, C., & Güney, G. (2020) · Archives of Insect Biochemistry and Physiology · doi:10.1002/arch.21682 · Cited by 222

Elevated miR-155 Promotes Inflammation in Cystic Fibrosis by Driving Hyperexpression of Interleukin-8

Bhattacharyya, S., Balakathiresan, N. S., Dalgard, C. L., Gutti, U., Armistead, D. L., Cathy, J., Srivastava, M., Pollard, H. B., & Biswas, R. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.198390 · Cited by 221

Toxicogenomics of non-viral drug delivery systems for RNAi: Potential impact on siRNA-mediated gene silencing activity and specificity

Akhtar, S., & Benter, I. F. (2007) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2007.03.010 · Cited by 222

Suppression of hepatitis B virus replication by microRNA-199a-3p and microRNA-210

Zhang, G., Li, Y., Zheng, S., Liu, M., Li, X., & Tang, H. (2010) · Antiviral Research · doi:10.1016/j.antiviral.2010.08.008 · Cited by 221

A microRNA cluster as a target of genomic amplification in malignant lymphoma

Tagawa, H., & Seto, M. (2005) · Leukemia · doi:10.1038/sj.leu.2403942 · Cited by 221

CHANGES IN microRNA (miR) PROFILE AND EFFECTS OF miR‐320 IN INSULIN‐RESISTANT 3T3‐L1 ADIPOCYTES

Ling, H., Ou, H., Feng, S., Zhang, X., Tuo, Q., Chen, L., Zhu, B., Gao, Z., Tang, C., Yin, W., et al. (2009) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/j.1440-1681.2009.05207.x · Cited by 221

Lethal-7 is down-regulated by the hepatitis B virus x protein and targets signal transducer and activator of transcription 3

Wang, Y., Lu, Y., Toh, S. T., Sung, W.-K. K., Tan, P. B. O., Chow, P. K. H., Chung, A. Y. F., Jooi, L. L. P., & Lee, C. G. L. (2010) · Journal of Hepatology · doi:10.1016/j.jhep.2009.12.043 · Cited by 221

Hormonal Regulation of MicroRNA Expression in Periovulatory Mouse Mural Granulosa Cells1

Fiedler, S. D., Carletti, M. Z., Hong, X., & Christenson, L. K. (2008) · Biology of Reproduction · doi:10.1095/biolreprod.108.069690 · Cited by 221

MicroRNA-513 Regulates B7-H1 Translation and Is Involved in IFN-γ-Induced B7-H1 Expression in Cholangiocytes

Gong, A., Zhou, R., Hu, G., Li, X., Splinter, P. L., O’Hara, S. P., LaRusso, N. F., Soukup, G. A., Dong, H., & Chen, X. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.182.3.1325 · Cited by 220

Porphyrin and Heme Metabolism and the Porphyrias

Bonkovsky, H. L., Guo, J., Hou, W., Li, T., Narang, T. K., & Thapar, M. (2012) · Comprehensive physiology · doi:10.1002/cphy.c120006 · Cited by 220

Liver fibrosis causes downregulation of miRNA-150 and miRNA-194 in hepatic stellate cells, and their overexpression causes decreased stellate cell activation

Venugopal, S. K., Jiang, J. X., Kim, T.-H., Li, Y., Wang, S., Torok, N. J., Wu, J., & Zern, M. Α. (2009) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00220.2009 · Cited by 220

MicroRNA-143 and -145 in Colon Cancer

Akao, Y., Nakagawa, Y., & Naoe, T. (2007) · DNA and Cell Biology · doi:10.1089/dna.2006.0550 · Cited by 220

Acceleration of muscle regeneration by local injection of muscle‐specific microRNAs in rat skeletal muscle injury model

Nakasa, T., Ishikawa, M., Shi, M., Shibuya, H., Adachi, N., & Ochi, M. (2009) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2009.00898.x · Cited by 220

MicroRNA-500 as a potential diagnostic marker for hepatocellular carcinoma

Yamamoto, Y., Kosaka, N., Tanaka, M., Koizumi, F., Kanai, Y., Mizutani, T., Murakami, Y., Kuroda, M., Miyajima, A., Kato, T., et al. (2009) · Biomarkers · doi:10.3109/13547500903150771 · Cited by 220

Clinical Outcome Prediction by MicroRNAs in Human Cancer: A Systematic Review

Nair, V. S., Maeda, L. S., & Ioannidis, J. P. A. (2012) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/djs027 · Cited by 220

MicroRNA-155 is essential for TH2-mediated allergen-induced eosinophilic inflammation in the lung

Malmhäll, C., Alawieh, S., Lü, Y., Sjöstrand, M., Bossios, A., Eldh, M., & Rådinger, M. (2013) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2013.11.008 · Cited by 220

Bioinformatic tools for microRNA dissection

Akhtar, M. M., Micolucci, L., Islam, M. S., Olivieri, F., & Procopio, A. D. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv1221 · Cited by 220

Impact of Alcohol Abuse on the Adaptive Immune System

Pasala, S. (2015) · Alcohol research · doi:10.35946/arcr.v37.2.04 · Cited by 220

In Situ Amplification‐Based Imaging of RNA in Living Cells

Qing, Z., Xu, J., Hu, J., Zheng, J., He, L., Zou, Z., Yang, S., Tan, W., & Yang, R. (2019) · Angewandte Chemie International Edition · doi:10.1002/anie.201812449 · Cited by 220

Identification of miR-130a, miR-27b and miR-210 as serum biomarkers for atherosclerosis obliterans

Li, T., Cao, H., Zhuang, J., Wan, J., Guan, M., Yu, B., Li, X., & Zhang, W. (2010) · Clinica Chimica Acta · doi:10.1016/j.cca.2010.09.029 · Cited by 219

Mechanosensing and Mechanoregulation of Endothelial Cell Functions

Fang, Y. H., Wu, D., & Birukov, K. G. (2019) · Comprehensive physiology · doi:10.1002/cphy.c180020 · Cited by 222

Maternal Microbiota, Early Life Colonization and Breast Milk Drive Immune Development in the Newborn

Kalbermatter, C., Trigo, N. F., Christensen, S., & Ganal-Vonarburg, S. C. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.683022 · Cited by 220

MicroRNAs in kidney injury and disease

Mahtal, N., Lenoir, O., Tinel, C., Anglicheau, D., & Tharaux, P. (2022) · Nature Reviews Nephrology · doi:10.1038/s41581-022-00608-6 · Cited by 219

Recent advancement and strategy on bio-hydrogen production from photosynthetic microalgae

Anwar, M., Lou, S., Chen, L., Li, H., & Hu, Z. (2019) · Bioresource Technology · doi:10.1016/j.biortech.2019.121972 · Cited by 218

MicroRNA-binding viral protein interferes with Arabidopsis development

Padmanabhan, C., Ramachandran, V., & Fauquet, C. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504439102 · Cited by 218

Genome-scale spatiotemporal analysis of Caenorhabditis elegans microRNA promoter activityPreprint

Martinez, N. J., Ow, M. C., Reece-Hoyes, J. S., Barrasa, M. I., Ambros, V., & Walhout, A. J. M. (2008) · Genome Research · doi:10.1101/gr.083055.108 · Cited by 218

An antagomir to microRNA Let7f promotes neuroprotection in an ischemic stroke model

Selvamani, A., Sathyan, P., Miranda, R. C., & Sohrabji, F. (2012) · PLoS ONE · doi:10.1371/journal.pone.0032662 · Cited by 217

Control of Cholesterol Metabolism and Plasma High-Density Lipoprotein Levels by microRNA-144

Ramírez, C. M., Rotllan, N., Vlassov, A. V., Dávalos, A., Li, M., Goedeke, L., Aranda, J. F., Cirera-Salinas, D., Araldi, E., Salerno, A., et al. (2013) · Circulation Research · doi:10.1161/circresaha.112.300626 · Cited by 217

MicroRNAs: Biogenesis and Molecular Functions

Liu, X., Fortin, K., & Mourelatos, Z. (2008) · Brain Pathology · doi:10.1111/j.1750-3639.2007.00121.x · Cited by 218

MicroRNA-146a and Human Disease

Li, L., Chen, X.-P., & Li, Y.-J. (2010) · Scandinavian Journal of Immunology · doi:10.1111/j.1365-3083.2010.02383.x · Cited by 217

Altered expression of miR‐17‐5p in CD4+ lymphocytes of relapsing–remitting multiple sclerosis patients

Lindberg, R. L. P., Hoffmann, F., Mehling, M., Kühle, J., & Kappos, L. (2010) · European Journal of Immunology · doi:10.1002/eji.200940032 · Cited by 217

Systematic identification of microRNA functions by combining target prediction and expression profiling

Wang, X. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkl068 · Cited by 217

Serum microRNA profiling and breast cancer risk: the use of miR-484/191 as endogenous controls

Hu, Z., Dong, J., Wang, L., Ma, H., Liu, J., Zhao, Y., Tang, J., Chen, X., Dai, J., Wei, Q., et al. (2012) · Carcinogenesis · doi:10.1093/carcin/bgs030 · Cited by 217

Improving microRNA target prediction by modeling with unambiguously identified microRNA-target pairs from CLIP-ligation studies

Wang, X. (2016) · Bioinformatics · doi:10.1093/bioinformatics/btw002 · Cited by 217

MicroRNA Therapeutics in Cancer: Current Advances and Challenges

Sayed, S. R. E., Cristante, J., Guyon, L., Denis, J., Chabre, O., & Cherradi, N. (2021) · Cancers · doi:10.3390/cancers13112680 · Cited by 217

Three-Mode Electrochemical Sensing of Ultralow MicroRNA Levels

Labib, M., Khan, N., Ghobadloo, S. M., Cheng, J., Pezacki, J. P., & Berezovski, M. V. (2013) · Journal of the American Chemical Society · doi:10.1021/ja308216z · Cited by 216

Upregulation of miR-22 Promotes Osteogenic Differentiation and Inhibits Adipogenic Differentiation of Human Adipose Tissue-Derived Mesenchymal Stem Cells by Repressing HDAC6 Protein Expression

HUANG, S. H., Wang, S., Bian, C., Yang, Z., Zhou, H., Zeng, Y. C., Li, H., Han, Q., & Zhao, R. C. (2012) · Stem Cells and Development · doi:10.1089/scd.2012.0014 · Cited by 216

Hepatocyte-derived MicroRNAs as Serum Biomarkers of Hepatic Injury and Rejection after Liver Transplantation

Farid, W. R. R., Pan, Q., van der Meer, A. J. P., de Ruiter, P. E., Ramakrishnaiah, V., de Jonge, J., Kwekkeboom, J., Janssen, H. L. A., Metselaar, H. J., Tilanus, H. W., et al. (2011) · Liver Transplantation · doi:10.1002/lt.22438 · Cited by 216

microRNAs in Inflammation

Sonkoly, E., & Pivarcsi, A. (2009) · International Reviews of Immunology · doi:10.3109/08830180903208303 · Cited by 216

Genome-wide survey of tissue-specific microRNA and transcription factor regulatory networks in 12 tissues.

Guo, Z., Maki, M., Ding, R., Yang, Y., zhang, B., & Xiong, L. (2014) · Scientific Reports · doi:10.1038/srep05150 · Cited by 215

Cell-specific effects of miR-221/222 in vessels: Molecular mechanism and therapeutic application

Liu, X., Cheng, Y., Yang, J., Xu, L., & Zhang, C. (2011) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2011.11.008 · Cited by 214

microRNA expression profile in undifferentiated gastric cancer

Ishiguro (1992) · International Journal of Oncology · doi:10.3892/ijo_00000179 · Cited by 214

Endothelial microRNAs regulating the NF‐κB pathway and cell adhesion molecules during inflammation

Zhong, L., Simard, M. J., & Huot, J. (2018) · The FASEB Journal · doi:10.1096/fj.201701536r · Cited by 214

Mechanistic Role of MicroRNA-146a in Endotoxin-Induced Differential Cross-Regulation of TLR Signaling

Nahid, M. A., Satoh, M., & Chan, E. K. L. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.1002311 · Cited by 213

Milk is not just food but most likely a genetic transfection system activating mTORC1 signaling for postnatal growth

Melnik, B. C., John, S. M., & Schmitz, G. (2013) · Nutrition Journal · doi:10.1186/1475-2891-12-103 · Cited by 213

Phthalate exposure and long-term epigenomic consequences: a review

Dutta, S., Haggerty, D. K., Rappolee, D. A., & Ruden, D. M. (2020) · Frontiers in Genetics · doi:10.3389/fgene.2020.00405 · Cited by 212

Ago–TNRC6 triggers microRNA-mediated decay by promoting two deadenylation steps

Chen, C. A., Zheng, D., Xia, Z., & Shyu, A. (2009) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1709 · Cited by 212

myc maintains embryonic stem cell pluripotency and self-renewal

Varlakhanova, N. V., Cotterman, R. F., de Vries, W. N., Morgan, J., Donahue, L. R., Murray, S. A., Knowles, B. B., & Knoepfler, P. S. (2010) · Differentiation · doi:10.1016/j.diff.2010.05.001 · Cited by 212

NF-kappaB p65-Dependent Transactivation of miRNA Genes following Cryptosporidium parvum Infection Stimulates Epithelial Cell Immune Responses

Zhou, R., Hu, G., Liu, J., Gong, A.-Y., Drescher, K. M., & Chen, X. (2009) · PLoS Pathogens · doi:10.1371/journal.ppat.1000681 · Cited by 212

PmiREN: a comprehensive encyclopedia of plant miRNAs

Guo, Z., Kuang, Z., Wang, Y., Zhao, Y., Tao, Y., Chen, C., Yang, J., Lu, X., Chen, H., Wang, T., et al. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz894 · Cited by 212

Role of epithelial-mesenchymal transition in gastric cancer initiation and progression

Peng, Z. (2014) · World Journal of Gastroenterology · doi:10.3748/wjg.v20.i18.5403 · Cited by 211

MicroRNA regulates human vitamin D receptor

Mohri, T., Nakajima, M., Takagi, S., Komagata, S., & Yokoi, T. (2009) · International Journal of Cancer · doi:10.1002/ijc.24459 · Cited by 211

Mouse miRNA-709 directly regulates miRNA-15a/16-1 biogenesis at the posttranscriptional level in the nucleus: evidence for a microRNA hierarchy system

Tang, R., Li, L., Zhu, D., Hou, D., Cao, T., Gu, H., Zhang, J., Chen, J., Zhang, C., & Zen, K. (2011) · Cell Research · doi:10.1038/cr.2011.137 · Cited by 211

Functions of MicroRNAs in Animals

Shao, R. (2005) · Yixue fenzi shengwuxue zazhi

Conservation and Evolution of microRNAs in Animals

LIANG, Y., Zhang, S., Luo, Y., & Zhang, Q. (2012) · Scientia Sinica Vitae · doi:10.1360/052011-594 · Cited by 3

Micro RNA s in Animal Development

Mansfield, J. H. (2010) · Wiley eBooks · doi:10.1002/9780470015902.a0021489 · Cited by 31

MicroRNA in cell differentiation and development

Shi, Y., & Jin, Y. (2009) · Science in China Series C Life Sciences · doi:10.1007/s11427-009-0040-5 · Cited by 69

The multitudinous role of microRNAs in various biological systems

Keerthana, R., Kumar, S., & Perumal, P. (2013) · Journal of Pharmacy Research · doi:10.1016/j.jopr.2013.02.033 · Cited by 2